Package 68788-8771-3

Brand: omeprazole

Generic: omeprazole
NDC Package

Package Facts

Identity

Package NDC 68788-8771-3
Digits Only 6878887713
Product NDC 68788-8771
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-3)

Marketing

Marketing Status
Marketed Since 2024-11-20
Brand omeprazole
Generic omeprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c3183e18-e844-49e6-8546-270232604cbf", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9"], "rxcui": ["200329"], "spl_set_id": ["288bdd5e-a0ac-4c5c-abe0-93183a28dcdd"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-1)", "package_ndc": "68788-8771-1", "marketing_start_date": "20241120"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-3)", "package_ndc": "68788-8771-3", "marketing_start_date": "20241120"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-6)", "package_ndc": "68788-8771-6", "marketing_start_date": "20241120"}, {"sample": false, "description": "120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-8)", "package_ndc": "68788-8771-8", "marketing_start_date": "20241120"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-9)", "package_ndc": "68788-8771-9", "marketing_start_date": "20241120"}], "brand_name": "Omeprazole", "product_id": "68788-8771_c3183e18-e844-49e6-8546-270232604cbf", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68788-8771", "generic_name": "Omeprazole", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "40 mg/1"}], "application_number": "ANDA078490", "marketing_category": "ANDA", "marketing_start_date": "20241120", "listing_expiration_date": "20271231"}